A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612999



Internal ID16400408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:290670..526772hg38UCSC Ensembl
Innerchr9:290670..526772hg19UCSC Ensembl
Innerchr9:280670..516772hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38236103
hg19236103
hg18236103
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12451n54
Supporting Variantsnssv1125858
Samples
Known GenesDOCK8, KANK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612999
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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